QA Batch Record Reviewer_CH

Description

Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing.

• Review paper-based executed batch records within the specified timeframe.
• Track, report and monitor batch record review and other relevant critical metrics to ensure on-time batch release.
• Raise meetings with Ops related observations in a timely manner.

• Professional experience in GMP production environment, quality procedures and SOP execution and/or Bachelor’s/Master’s Degree or equivalent experience.
• Preferred area of study:
  Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or equivalent scientific degree.
• Experience in batch record review is highly preferred.
• GMP experience (min. 2 years)
• Great communication skills

• On‑Site in Visp (no home office) – Paper based
• Business fluent German is a MUST
• English preferred
• Due to Swiss Employment regulations, for this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport.

Interested? I look forward to receiving your application!

Welcome to a leading company in the pharmaceutical manufacturing industry, recognized for its commitment to quality, compliance, and operational excellence. We offer you the opportunity to work in a highly regulated and professional environment where your expertise is valued and your attention to detail makes a real impact on patient safety and product quality.

Our organization places strong emphasis on GMP standards, teamwork, and continuous improvement. You will collaborate closely with cross‑functional teams to ensure timely and compliant batch release while contributing to a culture built on precision, accountability, and open communication.

Join our dedicated team in Visp and help ensure the highest standards in pharmaceutical manufacturing.